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        "NM_001135146.2:c.923C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001128618.1:p.Thr308Met",
        "hgvsWellDefined": "NP_001128618.1:p.Thr308Met"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS663642",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000356736.5:c.923C>T"
          },
          "RefSeq": {
            "hgvs": "NM_001135146.2:c.923C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000349174.4:p.Thr308Met"
          },
          "RefSeq": {
            "hgvs": "NP_001128618.1:p.Thr308Met"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2825788967",
      "coordinates": [
        {
          "allele": "T",
          "end": 767,
          "referenceAllele": "C",
          "start": 766
        }
      ],
      "gene": "http://reg.genome.network/gene/GN020862",
      "geneNCBI_id": 64116,
      "geneSymbol": "SLC39A8",
      "hgvs": [
        "NM_001135148.2:c.722C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001128620.1:p.Thr241Met",
        "hgvsWellDefined": "NP_001128620.1:p.Thr241Met"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS712418"
    }
  ],
  "type": "nucleotide"
}